Canonical Allele Identifier: PA891848823
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 581675
ClinVar RCV Id: RCV000705576 RCV001830560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile86Val
CA4450675
NM_000492.4:c.256A>G